Experienced Clinical Research Associate

IQVIA, Inc.; Reading; On-site; GBP 35,000 - 55,000; Full time

Job summary

An established industry player is seeking experienced Clinical Research Associates to join their mission of improving global health. In this pivotal role, you will manage site operations, ensuring compliance with Good Clinical Practice and ICH guidelines while supporting clinical trials. You'll work closely with healthcare sites to enhance patient recruitment and provide essential training. This is a unique opportunity to contribute to groundbreaking medical advancements while being part of a diverse and innovative team dedicated to making a significant impact in healthcare. If you're passionate about clinical research and eager to grow your career, this role is for you.

Qualifications

• Experience in independent on-site monitoring in the UK.
• In-depth knowledge of GCP and ICH guidelines.

Responsibilities

• Manage site selection, initiation, and monitoring visits.
• Train and mentor junior team members as needed.

Skills

On-site Monitoring

Good Clinical Practice (GCP)

International Conference on Harmonization (ICH)

Site Management

Protocol Training

Education

Life Science Degree

Equivalent Industry Experience

Job description

IQVIA Clinical FSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK to join us on our mission to help create a healthier world.

By joining our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

Responsibilities

• Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits) in partnership with a single-sponsor.
• Working with sites to adapt, drive and track subject recruitment plan.
• Providing protocol and study training to assigned sites.
• Creating and maintaining monitoring visit reports and action plans.
• If appropriate, co-monitoring, training and mentoring junior members of the team.

Requirements

• Experience of independent on-site monitoring in the UK.
• In-depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Life science degree educated or equivalent industry experience.
• Flexibility to travel to sites as required.

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

*Please note - this role is not eligible for UK visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com